FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

707608003: Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3030814014 Jalili syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3030832014 Amelogenesis imperfecta co-occurrent with cone rod dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3030889013 Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3030814014 Jalili syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3030832014 Amelogenesis imperfecta co-occurrent with cone rod dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3030832014 Amelogenesis imperfecta co-occurrent with cone rod dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3030889013 Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3030889013 Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
519611000274119 Zapfen-Stäbchen-Dystrophie - Amelogenesis imperfecta de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3415941001000119 Jalili-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5975821000241110 amélogenèse imparfaite concomitante d'une dystrophie des cônes et des bâtonnets fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5975831000241112 syndrome de Jalili fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5975821000241110 amélogenèse imparfaite concomitante d'une dystrophie des cônes et des bâtonnets fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5975831000241112 syndrome de Jalili fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
519611000274119 Zapfen-Stäbchen-Dystrophie - Amelogenesis imperfecta de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3415941001000119 Jalili-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Is a Hereditary retinal dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Is a Amelogenesis imperfecta (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Finding site Enamel structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start